抄録
We previously developed a lymphocyte microwell-array system, which effectively detects antigen-specific B-cells by monitoring intracellular Ca 2+ mobilization at the single-cell level with a fluorescent Ca 2+ indicator, fluo-4. However, it is difficult for the system to perform time-lapse monitoring. Here, we developed a novel method, a lymphocyte microwell-array chip system equipped with a charge-coupled device (CCD) time-lapse scanner (MAC-CCD system), for monitoring intracellular Ca 2+ mobilization. The MAC-CCD system is able to monitor intracellular Ca2+ mobilization of more than 15,000-20,000 individual live B-cells every 10 s. In addition, we adopted a correlation method in a MAC-CCD system, which enabled us to detect B-cells with a frequency of as few as 0.046%. Furthermore, we succeeded in obtaining six influenza nucleoprotein-specific human monoclonal antibodies from the peripheral blood of influenza-vaccinated volunteers. These results demonstrate that the MAC-CCD system with a correlation method could detect very rare antigen-specific B-cells.
本文言語 | 英語 |
---|---|
ページ(範囲) | 158-163 |
ページ数 | 6 |
ジャーナル | Lab on a Chip |
巻 | 9 |
号 | 1 |
DOI | |
出版ステータス | 出版済み - 2009 |
ASJC Scopus 主題領域
- バイオエンジニアリング
- 生化学
- 化学一般
- 生体医工学